Bupropion Hydrochloride
- Product NDC
- 50090-1768
- 11-digit product format
- 500901768
- Labeler code
- 50090
- Product ID
- 50090-1768_7256331b-bad4-4162-8267-1485ddc7cdc1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075932
- Marketing category
- ANDA
- Marketing start
- 2003-11-25
- Marketing end
- 0000-00-00
- Substance
- BUPROPION HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1768-2 | 50090176802 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-1768-2) | 2018-08-08 | 0000-00-00 | No | No | Current |